Clinical Research Professional / Senior Clinical Research Professional, Int

at  University of Cincinnati

Current UC employees must apply internally via SuccessFactors > http://bit.ly/UCEMPL
Founded in 1819, the University of Cincinnati ranks among the nation’s best urban public research universities. Home to 53,235 students, more than 11,000 faculty and staff and 350,000+ living alumni, UC combines a Top 35 public research university with a physical setting The New York Times calls “the most ambitious campus design program in the country.”
With the launch of Next Lives Here, the Cincinnati Innovation District, a $100 million JobsOhio investment, three straight years of record enrollment, worldwide leadership in cooperative education, a dynamic academic health center and entry into the Big 12 Conference, UC’s momentum has never been stronger. UC’s annual budget stands at $1.85 billion, and its endowment totals nearly $1.8 billion.

REQUIRED EDUCATION

• Bachelor’s Degree must be in a related field.
• Five (5) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.

REQUIRED EXPERIENCE

One (1) year of related experience.
- OR -

REQUIRED EDUCATION

• Bachelor’s Degree must be in a related field.
• Seven (7) years of relevant work experience and/or other specialized training can be used in lieu of education requirement.

REQUIRED EXPERIENCE

Three (3) years of related experience.

ADDITIONAL QUALIFICATIONS CONSIDERED

Experience in an academic or clinical setting in the area of clinical specialization.

PHYSICAL REQUIREMENTS/WORK ENVIRONMENT

• Sitting - Continuously

• Plan and coordinate clinical research projects.
• Facilitates communication with participants, nurses, physicians, sponsors, and ancillary personnel to maintain project study flow.
• Coordinates, schedules, and conducts research visits according to Good Clinical Practice (GCP), protocol, and all applicable policies and procedures.
• Participates in the preparation and/or submission of study-related materials, such as case report forms, adverse event reports, regulatory documents, etc.
• Assists in the generation of data for proposals, reports, and manuscripts.
• May serve as a resource person or act as a consultant within area of clinical expertise.
• Perform related duties based on departmental need.
• This job description can be changed at any time.